Leclercq I A, Field J, Enriquez A, Farrell G C, Robertson G R
Storr Liver Unit, University of Sydney at Westmead Hospital, Westmead, NSW 2145, Australia.
Biochem Biophys Res Commun. 2000 Feb 16;268(2):337-44. doi: 10.1006/bbrc.2000.2125.
In this study we have analyzed the inducible as well as constitutive hepatic expression of Cyp2e1 in a genetic model of obesity and non-insulin dependent (type II) diabetes, the leptin-deficient ob/ob mouse. In obese mice, Cyp2e1 levels were decreased compared to lean littermates. Treatment with leptin increased hepatic Cyp2e1 in obese mice to the levels observed in lean animals, but failed to alter Cyp2e1 expression in lean animals. As expected, leptin also reduced food intake in treated mice compared to saline-treated controls. In obese mice pair-fed the reduced amount of food, there was a significant increase in Cyp2e1 mRNA but no increase in Cyp2e1 protein or enzyme activity. Fasting and administration of acetone and 4-methylpyrazole increased Cyp2e1 mRNA as well as protein and activity in both obese and lean mice. The present data indicate that while Cyp2e1 is still inducible in obese mice by xenobiotics and fasting, full constitutive expression of Cyp2e1 requires leptin to be present. This effect of leptin appears to be at least partly independent of the hypothalamic control of food intake.
在本研究中,我们分析了肥胖和非胰岛素依赖型(II型)糖尿病的基因模型——瘦素缺乏的ob/ob小鼠中Cyp2e1的诱导性及组成性肝脏表达。与瘦的同窝小鼠相比,肥胖小鼠的Cyp2e1水平降低。用瘦素治疗可使肥胖小鼠肝脏中的Cyp2e1增加至瘦动物中观察到的水平,但未能改变瘦动物中Cyp2e1的表达。正如预期的那样,与用生理盐水处理的对照组相比,瘦素还减少了接受治疗小鼠的食物摄入量。在给肥胖小鼠喂食减少量食物的情况下,Cyp2e1 mRNA显著增加,但Cyp2e1蛋白或酶活性没有增加。禁食以及给予丙酮和4-甲基吡唑可增加肥胖和瘦小鼠中Cyp2e1的mRNA以及蛋白和活性。目前的数据表明,虽然外源性物质和禁食仍可在肥胖小鼠中诱导Cyp2e1,但Cyp2e1的完全组成性表达需要有瘦素存在。瘦素的这种作用似乎至少部分独立于下丘脑对食物摄入的控制。